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contexts to structured domain(s) and, hence, enhance the DVL functional space associated with them? Is there a direction, order or hierarchy in the phosphorylation of individual S/T sites and clusters in DVL
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contexts to structured domain(s) and, hence, enhance the DVL functional space associated with them? Is there a direction, order or hierarchy in the phosphorylation of individual S/T sites and clusters in DVL
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the context of translation control and cotranslational processes. We use methods of molecular biology, heterologous protein expression and purification, human tissue cultures, and structural biology methods
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